MX2019013003A - Dissociation of a 1,4-bis (4-phenoxybenzoylbenzene) - lewis acid complex in an aqueous solution. - Google Patents
Dissociation of a 1,4-bis (4-phenoxybenzoylbenzene) - lewis acid complex in an aqueous solution.Info
- Publication number
- MX2019013003A MX2019013003A MX2019013003A MX2019013003A MX2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A MX 2019013003 A MX2019013003 A MX 2019013003A
- Authority
- MX
- Mexico
- Prior art keywords
- phenoxybenzoylbenzene
- bis
- lewis acid
- aqueous solution
- dissociation
- Prior art date
Links
- ITVUPWDTDWMACZ-UHFFFAOYSA-N (4-phenoxyphenyl)-phenylmethanone Chemical compound C=1C=C(OC=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 ITVUPWDTDWMACZ-UHFFFAOYSA-N 0.000 title abstract 4
- 239000002841 Lewis acid Substances 0.000 title abstract 4
- 239000007864 aqueous solution Substances 0.000 title abstract 2
- 238000010494 dissociation reaction Methods 0.000 title 1
- 230000005593 dissociations Effects 0.000 title 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 2
- 150000007517 lewis acids Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 239000008346 aqueous phase Substances 0.000 abstract 1
- 239000007810 chemical reaction solvent Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000012074 organic phase Substances 0.000 abstract 1
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/79—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/80—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/85—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/127—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from carbon dioxide, carbonyl halide, carboxylic acids or their derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4012—Other compound (II) containing a ketone group, e.g. X-Ar-C(=O)-Ar-X for polyetherketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4093—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group characterised by the process or apparatus used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/34—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
- C08G2261/344—Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
- C08G2261/3442—Polyetherketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/40—Polymerisation processes
- C08G2261/45—Friedel-Crafts-type
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/62—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the nature of monomer used
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polyethers (AREA)
Abstract
The invention relates to a method for manufacturing 1,4-bis(4- phenoxybenzoylbenzene), comprising: -reacting terephthaloyl chloride with diphenyl ether in a reaction solvent and in the presence of a Lewis acid, so as to obtain a product mixture comprising a 1,4-bis(4-phenoxybenzoylbenzene)-Lewis acid complex; -putting the product mixture in contact with an aqueous solution, so as to obtain an aqueous phase containing the Lewis acid and an organic phase containing 1,4-bis(4-phenoxybenzoylbenzene).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17305581.5A EP3404011B1 (en) | 2017-05-18 | 2017-05-18 | Dissociation of a 1,4-bis(4-phenoxybenzoyl)benzene-lewis acid-complex in an aqueous solution |
| PCT/EP2018/063013 WO2018211045A1 (en) | 2017-05-18 | 2018-05-17 | Dissociation of a 1,4-bis (4-phenoxybenzoylbenzene) - lewis acid complex in an aqueous solution |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2019013003A true MX2019013003A (en) | 2020-02-05 |
Family
ID=58779047
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2019013003A MX2019013003A (en) | 2017-05-18 | 2018-05-17 | Dissociation of a 1,4-bis (4-phenoxybenzoylbenzene) - lewis acid complex in an aqueous solution. |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US20200109100A1 (en) |
| EP (2) | EP3404011B1 (en) |
| JP (1) | JP6795711B2 (en) |
| KR (1) | KR102196909B1 (en) |
| CN (1) | CN110650938A (en) |
| BR (1) | BR112019023478A2 (en) |
| CA (1) | CA3061558A1 (en) |
| ES (1) | ES2829267T3 (en) |
| MX (1) | MX2019013003A (en) |
| RU (1) | RU2019141830A (en) |
| WO (1) | WO2018211045A1 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3404008B1 (en) | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene at an elevated temperature |
| EP3404010B1 (en) | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene using substantially non-hydrolyzed terephthaloyl chloride |
| US10793500B2 (en) | 2017-05-16 | 2020-10-06 | Arkema France | Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent |
| EP3404012B1 (en) | 2017-05-18 | 2020-09-09 | Arkema France | Ripening of 1,4-bis (4-phenoxybenzoyl)benzene |
| ES2829267T3 (en) | 2017-05-18 | 2021-05-31 | Arkema France | Dissociation of a 1,4-bis (4-phenoxybenzoyl) benzene-Lewis acid complex in an aqueous solution |
| EP3650433B1 (en) | 2018-11-09 | 2024-04-24 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) at an elevated temperature |
| FR3110572B1 (en) * | 2020-05-19 | 2022-10-07 | Arkema France | Xanthene derivative, mixtures comprising it, method of manufacture and corresponding uses |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU445643A1 (en) | 1973-01-08 | 1974-10-05 | Институт Высокомолекулярных Соединений Ан Ссср | The method of obtaining 1,4-bis (4-phenoxybenzoyl) benzene |
| SU626555A1 (en) | 1973-03-05 | 1979-07-25 | Институт высокомолекулярных соединений | 1,4-bis-(4''-acetyl-4'-phenoxybenzoyl)-benzol as monomer for bend-strong and heat-resistant polymer |
| SU638588A1 (en) | 1977-06-28 | 1978-12-25 | Ярославский политехнический институт | Method of obtaining 1,4-bis-(4'-phenoxybenzoyl)-benzol |
| US4709007A (en) * | 1983-03-31 | 1987-11-24 | Raychem Corporation | Preparation of aromatic polymers |
| US4816556A (en) | 1985-02-22 | 1989-03-28 | E. I. Du Pont De Nemours And Company | Ordered polyetherketones |
| CA1246297A (en) * | 1985-03-11 | 1988-12-06 | Robert A. Clendinning | Process for preparing poly(aryl ether ketones) |
| US4716211A (en) | 1985-03-11 | 1987-12-29 | Amoco Corporation | Slurry process for producing high molecular weight crystalline polyaryletherketones |
| US4891167A (en) * | 1985-05-02 | 1990-01-02 | Amoco Corporation | Block polymers containing a poly(aryl ether ketone) and methods for their production |
| US4704448A (en) * | 1985-11-25 | 1987-11-03 | E. I. Du Pont De Nemours And Company | Copolyetherketones |
| US5137988A (en) * | 1986-07-25 | 1992-08-11 | Amoco Corporation | Amino-terminated poly(aryl ether ketones) |
| DE3789354T2 (en) | 1986-11-20 | 1994-08-04 | Asahi Chemical Ind | Aromatic polyether and process for making a polyether. |
| JPS63258923A (en) * | 1987-04-16 | 1988-10-26 | Asahi Chem Ind Co Ltd | Method for producing aromatic polyetherketone |
| US4826947A (en) | 1987-07-09 | 1989-05-02 | Raychem Corporation | Preparation of poly(arylene ether ketones) |
| US4794155A (en) * | 1987-08-26 | 1988-12-27 | The Dow Chemical Company | Process for forming arylether polymers |
| US4835319A (en) | 1987-11-09 | 1989-05-30 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a zeolite catalyst |
| US4827041A (en) * | 1988-03-10 | 1989-05-02 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with a perfluorosulfonyl resin catalyst |
| US4918237A (en) * | 1989-03-13 | 1990-04-17 | E. I. Du Pont De Nemours And Company | Process for the manufacture of 1,4-bis(4-phenoxybenzoyl)benzene with certain metal-containing catalysts |
| JPH04103517A (en) | 1990-08-22 | 1992-04-06 | Lion Corp | Hair cosmetic |
| US5258491A (en) * | 1992-09-04 | 1993-11-02 | Eastman Kodak Company | Process for preparation of a polyetherketone |
| GB9403944D0 (en) | 1994-03-02 | 1994-04-20 | Victrex Manufacturing Ltd | Aromatic polymers |
| FR2993567B1 (en) * | 2012-07-20 | 2015-09-25 | Arkema France | PROCESS FOR THE SYNTHESIS OF POLY-ARYL ETHER-KETONES |
| EP3404013B1 (en) * | 2017-05-18 | 2021-10-27 | Arkema France | Purification of 1,4-bis (4-phenoxybenzoyl)benzene by centrifugal filtration |
| EP3404012B1 (en) | 2017-05-18 | 2020-09-09 | Arkema France | Ripening of 1,4-bis (4-phenoxybenzoyl)benzene |
| ES2774725T3 (en) * | 2017-05-16 | 2020-07-22 | Arkema France | Method of manufacturing 1,4-bis (4-phenoxybenzoyl) benzene under supersaturated conditions |
| US10793500B2 (en) * | 2017-05-16 | 2020-10-06 | Arkema France | Dissociation of 1,4-bis (4-phenoxybenzoyl)benzene—Lewis acid complex in a protic solvent |
| EP3404010B1 (en) * | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene using substantially non-hydrolyzed terephthaloyl chloride |
| EP3404008B1 (en) * | 2017-05-16 | 2020-08-12 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoyl)benzene at an elevated temperature |
| ES2829267T3 (en) | 2017-05-18 | 2021-05-31 | Arkema France | Dissociation of a 1,4-bis (4-phenoxybenzoyl) benzene-Lewis acid complex in an aqueous solution |
| EP3438085A1 (en) * | 2017-08-04 | 2019-02-06 | Arkema France | Process for producing polyether ketone ketone |
| EP3650434A1 (en) | 2018-11-09 | 2020-05-13 | Arkema France | Method for manufacturing 1,4-bis (4-phenoxybenzoylbenzene) using substantially non-hydrolyzed terephthaloyl chloride |
-
2017
- 2017-05-18 ES ES17305581T patent/ES2829267T3/en active Active
- 2017-05-18 EP EP17305581.5A patent/EP3404011B1/en active Active
-
2018
- 2018-05-17 CN CN201880032786.1A patent/CN110650938A/en active Pending
- 2018-05-17 US US16/613,600 patent/US20200109100A1/en not_active Abandoned
- 2018-05-17 BR BR112019023478-0A patent/BR112019023478A2/en not_active Application Discontinuation
- 2018-05-17 WO PCT/EP2018/063013 patent/WO2018211045A1/en not_active Ceased
- 2018-05-17 RU RU2019141830A patent/RU2019141830A/en not_active Application Discontinuation
- 2018-05-17 EP EP18724254.0A patent/EP3625205A1/en not_active Withdrawn
- 2018-05-17 CA CA3061558A patent/CA3061558A1/en not_active Abandoned
- 2018-05-17 US US15/982,625 patent/US11358924B2/en active Active
- 2018-05-17 JP JP2019563519A patent/JP6795711B2/en not_active Expired - Fee Related
- 2018-05-17 KR KR1020197036781A patent/KR102196909B1/en active Active
- 2018-05-17 MX MX2019013003A patent/MX2019013003A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR102196909B1 (en) | 2020-12-30 |
| CN110650938A (en) | 2020-01-03 |
| BR112019023478A2 (en) | 2020-06-30 |
| US11358924B2 (en) | 2022-06-14 |
| US20180334420A1 (en) | 2018-11-22 |
| CA3061558A1 (en) | 2018-11-22 |
| RU2019141830A3 (en) | 2021-06-18 |
| ES2829267T3 (en) | 2021-05-31 |
| US20200109100A1 (en) | 2020-04-09 |
| JP6795711B2 (en) | 2020-12-02 |
| KR20200003203A (en) | 2020-01-08 |
| JP2020520361A (en) | 2020-07-09 |
| RU2019141830A (en) | 2021-06-18 |
| EP3404011B1 (en) | 2020-08-26 |
| WO2018211045A1 (en) | 2018-11-22 |
| EP3625205A1 (en) | 2020-03-25 |
| EP3404011A1 (en) | 2018-11-21 |
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